US3012985A - Pelletized sulfur - Google Patents

Pelletized sulfur Download PDF

Info

Publication number
US3012985A
US3012985A US724258A US72425858A US3012985A US 3012985 A US3012985 A US 3012985A US 724258 A US724258 A US 724258A US 72425858 A US72425858 A US 72425858A US 3012985 A US3012985 A US 3012985A
Authority
US
United States
Prior art keywords
sulfur
parts
rubber
oil
pellets
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US724258A
Inventor
Zakheim Murray
James R Doonan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Stauffer Chemical Co
Original Assignee
Stauffer Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co
Priority to US724258A priority Critical patent/US3012985A/en
Application granted granted Critical
Publication of US3012985A publication Critical patent/US3012985A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/06Sulfur
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00Sulfur; Compounds thereof
    • C01B17/02Preparation of sulfur; Purification
    • C01B17/0237Converting into particles, e.g. by granulation, milling
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/08Ingredients agglomerated by treatment with a binding agent
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S524/00Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S524/925Natural rubber compositions having nonreactive materials, i.e. NRM, other than: carbon, silicon dioxide, glass titanium dioxide, water, hydrocarbon or halohydrocarbon
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S524/00Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S524/925Natural rubber compositions having nonreactive materials, i.e. NRM, other than: carbon, silicon dioxide, glass titanium dioxide, water, hydrocarbon or halohydrocarbon
    • Y10S524/926Natural rubber compositions having nonreactive materials, i.e. NRM, other than: carbon, silicon dioxide, glass titanium dioxide, water, hydrocarbon or halohydrocarbon with water as NRM, exemplified

Definitions

  • This invention relates to the provision of a pelleted sulfur product, the pellets so produced being stable and exhibiting a high degree of resistance against attritional losses in the form of dust, fines and other pellet fragments as the product is handled.
  • Sulfur as conventionally supplied in the form of a fine powder, is difiicult to handle since it is not free flowing and tends to plug the lines through which it is passed in numerous manufacturing operations. It also forms a fine dust in the atmosphere which presents a health as well as an explosion hazard.
  • attempts have heretofore been made to supply finely divided sulfur in the form of small pellets of one type or another. Many of the products so formed have utilized a relatively large percent of binding medium, thereby adding materially to product costs, while at the same time seriously degrading the quality of the product. Even aside from such factors, the pelleted sulfur materials hitherto available have been relatively friable and non-plastic; as a result, they have not held up well under handling, particularly after being stored for any appreciable length of time.
  • a further object is to provide a sulfur product which is plastic and otherwise adapted to be evenly worked into a mass of rubber as the latter is compounded and rolled.
  • the present invention is based on the discovery that the foregoing objects can readily be achieved by pelleting the powdered sulfur starting material with binder comprised of small but critical amounts of rubber latex, an oil, and a surface active agent acting to emulsify the oil and make the same compatible with the latex.
  • binder comprised of small but critical amounts of rubber latex, an oil, and a surface active agent acting to emulsify the oil and make the same compatible with the latex.
  • the pellets contain from about 1.1 to 1.25 parts of rubber latex, 0.25 to 1.5 parts oil, and a sufficient amount of the surface active agent to eifect proper emulsification of the oil component, good results normally being had by using 0.025 to 0.25 part per 100 parts of sulfur.
  • the pellets are formed by combining the sulfur and binder ingredients with water to form a paste which is then extruded or otherwise formed. into shapes of the desired size and configuration, and these shapes are then dried to provide the final pellet product.
  • These pellets are especially well adapted to be incorporated in any of the usual rubber mixes wherein sulfur is a necessary component, though, they are also employed with good results in preparing insecticide sprays, granular insecticides and fungicides, and the like.
  • any desired, finely divided sulfur can be pelleted in the fashion described above.
  • use can be, made of any of the rubber-makers sulfur grades such, for example, as those commonly designated as tire brand, tube brand, flowers of sulfur, and insoluble sulfur; these latter two sulfurs are characterized in having a substantial sulfur 3,012,935 Patented Dec. 1 2, 1961 content which is insoluble in carbon bisulfide.
  • pellets to be dissolved or dispersed in an appropriate vehicle for use in insecticidal spray applications or granular type insecticides or fungicides other grades of sulfur can be employed, as required.
  • the rubber latex component of the pellet is employed in the proportion of at least 0.1, part and normally in a range. of, from 0,.1' to 1.25, part per 100 parts by weight of sulfur.
  • Use of a latex'content below 0.1 part decreases the plasticity of the product and also results in a pelleted structure of unduly low stability.
  • such pellets, for lack of required plasticity are not readily accepted by the nip of the rubber mill and tend to jump therefrom, whereas those prepared with 0.1 part or more of latex smear out and disperse readily in the rubber in the mill.
  • the unsatisfactory stability qualities which characterize pellets prepared with less than 0.1 part latex are further evidenced by a large increase in the fines produced as the pellets are handled, particularly after storage periods of one or more months.
  • a preferred range for the latex component is from 0.25 to 1 part, while amounts larger than about 1.25 parts are not recommended since the expense of the binder is increased without olfering any further benefits from the product quality standpoint.
  • the use of amounts of latex larger than 1.25 parts is in no wise hampered as regards the quality of the pellets.
  • Rubber latices satisfactory for use in the present invention comprises those derived from either natural rubbers or the various types of synthetic rubbers such, for example, as acrylic rubbers, butadiene-acrylonitrile copolymers, butadiene-styrene rubbers, butadiene polymer, chloroprene rubbers, isobutylene rubbers, polyisobutyleneisoprene copolymers, silicone rubbers and polysulfide rubbers. Particularly good results have been obtained with rubber latices combining butadiene and styrene in the ratio of 70:30, respectively.
  • Rubber latices are normally available in the form of fine dispersions in an aqueous vehicle, or are capable of being so dispersed preparatory to being combined with sulfur and the other binder ingredients to form the pellets hereof, typical dispersions containing approximately 23' to 62 percent rubber in the latex.
  • the oil ingredient of the binder is employed in an amount of at least 0.25 part and normally of from about 0.25 to 1.5 part, per parts of sulfur. Pellets prepared with less than 0.25 part oil have little stability and are easily abraded and fractured. On the other hand, additions of oil beyond 1.25 parts do not alter the physical properties and. serve only to increase the cost of the product. While satisfactory results can be obtained by using various oils, such as pine tar oil, cottonseed oil, synthetic plasticizers such as butyl oleate and dioctyl phthalate, oils of the so-called process variety (highly refined petroleum oils manufactured expressly for plasticizing various rubbers) are employed in the preferred practice of this invention.
  • Coprol Oil B (Atlantic Refining Company), Circo Light Processing Oil (Sun Oil Company, and Sovaloid N (Socony Mobil Oil Co.).
  • Coprol Oil B has an A.P.I gravity at 60 F. of 23.5, and the S.S.U. Viscosity is at 100 F. and 39 at 210 F.
  • the surface-active agent employed is one which is capable of effectively emulsifying the oil and bringing about compatibility with the latex; in the sulfur-paste mixture, the amount of emulsifyer employed for this purpose generally falling into a range. of from about 0.025 to 0.25 part, per 100 parts of sulfur, or, expressed otherwise, per single part of oil.
  • Representative einul sifying agents'of the anionic. type which may be successfully employed in a practice of this invention include various alkyl aryl sulfonates such as Nacconol NRSF (Allied Chemical and Dye corporation), Tamol N (Rohm and Haas Company), Nekal BX-78 (General Aniline and Film Corporation), petroleum sulfonates such as Petronate HL (L.
  • fatty acid sulfates such as Duponol ME (du Pont Co.) and Orvus W A Paste (Proctor and Gamble Company).
  • emulsifiers of the non-ionic type e.g., Atlas 1256, a polyoxyethylene sorbitol ester of a higher fatty acid, as marketed by Atlas Powder Company, and Triton X-100, an alkyl aryl polyether alcohol, as marketed by Rohm and Haas Co.
  • the recommended practice is to add sufficient water to the mixture of sulfur and additives to form a cohesive agglomerate, or heavy paste which can then be divided by a practice of conventional extrusion or screening methods into small pieces having the shape desired in the finished pellet.
  • the quantity of water required is of the order of 15-25 parts per 100 parts of sulfur.
  • pastes were prepared containing water parts), rubber-makers sulfur (100 parts), emulsifier (Atlas 1256) 0.1 part, oil (Coprol ()il B) 1.0 part, and rubber latex (either Pliolite Latex 2105 or Polyco 397-70 NS, both 70:30 butadiene-styrene rubbers) in varying proportions, i.e., 0.1, 0.25, 0.5 and 1.0, respectively.
  • These parts by weight of the latex are on a dry weight basis and do not take into account the amount of water (about 60 percent) and other non-rubber materials present in the commercial product.
  • As a control As a control,
  • the amount of fines produced from pellets dried at 50 C. and 70 C. was substantially the same as from pellets dried at 90 C.
  • the various paste compositions prepared were forced through an 8-mesh screen, the extrudate being cut from the screen and allowed to drop in a pan.
  • the pan was then oscillated in a circular motion, and within several moments spherical or oval pellets apuproximately diameter were formed. These wet pellets were then dried at a temperature of 90 C.
  • rubber and rubber latex are employed somewhat interchangeably, reference being had, in any event, to a product formed by the addition of a rubber latex material, as described above.
  • a pelleted sulfur product comprising predominantly sulfur and containing from about 0.1 to 1.25 parts rub ber per parts sulfur, said rubber being selected from the group consisting of natural rubber, butadiene-acrylonitrile copolymers, butadiene-styrene rubbers, rubbery chloroprene polymers and isobutylene-isoprene co-polymers and mixtures thereof, from 0.025 to 0.25 part of a surface active agent selected from the group consisting of anionic and non-ionic surface active agents per 100 parts sulfur and at least 0.25 part hydrocarbon oil per 100 parts sulfur, all parts being by weight.
  • a pelleted sulfur product containing from about 0.1 to 1.25 parts of rubber per 100 parts sulfur, said rubber being selected from the group consisting of natural rubber, butadiene-acrylonitrile co-polymers, butadiene-styreue rubbers, rubbery chloroprene polymers and isobutylene-isoprene co-polymers, and mixtures thereof and from 0.025 to 0.25 part of a surface active agent selected from the group consisting of anionic and non-ionic surface active agents per 100 parts of sulfur and 0.25 to 1.5 parts of a hydrocarbon oil per 100 parts of sulfur, all parts being by weight.
  • a process for the production of sulfur in the form of pellets having good plasticity and stability characteristics which comprises admixing 100 parts of powdered sulfur, 0.1 to 1.25 parts rubber latex, said latex being selected from the group consisting of natural rubber, butadiene-acrylonitrile co-polymers, butadiene-styrene rubbers, rubbery chlorcprene polymers and isobutylene-isoprene co-polymers, and mixtures thereof, 0.25 to 1.5 parts hydrocarbon oil and a sufiicient amount of a surface active agent selected from the group consisting of anionic and non-ionic surface active agents to emulsify the oii and with water in amount necessary to form a paste; forming References Cited in the file of this patent UNITED STATES PATENTS 1,871,038 Cadwell Aug. 9, 1932 2,069,710 Missbach Feb. 2, 1937 2,640,088 Glenn et a1 May 26, 1953 OTHER REFERENCES Hancock: Industrial

Description

United States Patent 3,012,985 PELLETIZED SULFUR Murray Zakheim, Yonkers, and James R. Doonan, Mount Vernon, N.Y., assignors to Stautfer Chemical Company, a corporation of Delaware No Drawing. Filed Mar. 27, 1958, er. No. 724,258 8 Claims. (Cl. 260-33.6)
This invention relates to the provision of a pelleted sulfur product, the pellets so produced being stable and exhibiting a high degree of resistance against attritional losses in the form of dust, fines and other pellet fragments as the product is handled.
Sulfur, as conventionally supplied in the form of a fine powder, is difiicult to handle since it is not free flowing and tends to plug the lines through which it is passed in numerous manufacturing operations. It also forms a fine dust in the atmosphere which presents a health as well as an explosion hazard. For these and other reasons attempts have heretofore been made to supply finely divided sulfur in the form of small pellets of one type or another. Many of the products so formed have utilized a relatively large percent of binding medium, thereby adding materially to product costs, while at the same time seriously degrading the quality of the product. Even aside from such factors, the pelleted sulfur materials hitherto available have been relatively friable and non-plastic; as a result, they have not held up well under handling, particularly after being stored for any appreciable length of time.
It is an object of this invention to provide a pelleted sulfur product which is free of the foregoing disadvantages, and contains a very small proportion of non-sulfur ingredients, and which is highly resistant to attritional loss even with severe handling and after prolonged storage.
A further object is to provide a sulfur product which is plastic and otherwise adapted to be evenly worked into a mass of rubber as the latter is compounded and rolled. The nature of still other objects of the invention will be apparent from a consideration of the descriptive portion to follow.
The present invention is based on the discovery that the foregoing objects can readily be achieved by pelleting the powdered sulfur starting material with binder comprised of small but critical amounts of rubber latex, an oil, and a surface active agent acting to emulsify the oil and make the same compatible with the latex. On a dry weight basis, the pellets contain from about 1.1 to 1.25 parts of rubber latex, 0.25 to 1.5 parts oil, and a sufficient amount of the surface active agent to eifect proper emulsification of the oil component, good results normally being had by using 0.025 to 0.25 part per 100 parts of sulfur.
The pellets are formed by combining the sulfur and binder ingredients with water to form a paste which is then extruded or otherwise formed. into shapes of the desired size and configuration, and these shapes are then dried to provide the final pellet product. These pellets are especially well adapted to be incorporated in any of the usual rubber mixes wherein sulfur is a necessary component, though, they are also employed with good results in preparing insecticide sprays, granular insecticides and fungicides, and the like.
Any desired, finely divided sulfur can be pelleted in the fashion described above. Thus, in the case of pellets which are to be incorporated in a mass of rubber to provide the sulfur ingredient thereof, use can be, made of any of the rubber-makers sulfur grades such, for example, as those commonly designated as tire brand, tube brand, flowers of sulfur, and insoluble sulfur; these latter two sulfurs are characterized in having a substantial sulfur 3,012,935 Patented Dec. 1 2, 1961 content which is insoluble in carbon bisulfide. With pellets to be dissolved or dispersed in an appropriate vehicle for use in insecticidal spray applications or granular type insecticides or fungicides, other grades of sulfur can be employed, as required.
The rubber latex component of the pellet, as, noted above, is employed in the proportion of at least 0.1, part and normally in a range. of, from 0,.1' to 1.25, part per 100 parts by weight of sulfur. Use of a latex'content below 0.1 part decreases the plasticity of the product and also results in a pelleted structure of unduly low stability. Thus, such pellets, for lack of required plasticity are not readily accepted by the nip of the rubber mill and tend to jump therefrom, whereas those prepared with 0.1 part or more of latex smear out and disperse readily in the rubber in the mill.
The unsatisfactory stability qualities which characterize pellets prepared with less than 0.1 part latex are further evidenced by a large increase in the fines produced as the pellets are handled, particularly after storage periods of one or more months. A preferred range for the latex component is from 0.25 to 1 part, while amounts larger than about 1.25 parts are not recommended since the expense of the binder is increased without olfering any further benefits from the product quality standpoint. However, the use of amounts of latex larger than 1.25 parts is in no wise hampered as regards the quality of the pellets.
Rubber latices satisfactory for use in the present invention comprises those derived from either natural rubbers or the various types of synthetic rubbers such, for example, as acrylic rubbers, butadiene-acrylonitrile copolymers, butadiene-styrene rubbers, butadiene polymer, chloroprene rubbers, isobutylene rubbers, polyisobutyleneisoprene copolymers, silicone rubbers and polysulfide rubbers. Particularly good results have been obtained with rubber latices combining butadiene and styrene in the ratio of 70:30, respectively. These and other rubber latices are normally available in the form of fine dispersions in an aqueous vehicle, or are capable of being so dispersed preparatory to being combined with sulfur and the other binder ingredients to form the pellets hereof, typical dispersions containing approximately 23' to 62 percent rubber in the latex.
The oil ingredient of the binder is employed in an amount of at least 0.25 part and normally of from about 0.25 to 1.5 part, per parts of sulfur. Pellets prepared with less than 0.25 part oil have little stability and are easily abraded and fractured. On the other hand, additions of oil beyond 1.25 parts do not alter the physical properties and. serve only to increase the cost of the product. While satisfactory results can be obtained by using various oils, such as pine tar oil, cottonseed oil, synthetic plasticizers such as butyl oleate and dioctyl phthalate, oils of the so-called process variety (highly refined petroleum oils manufactured expressly for plasticizing various rubbers) are employed in the preferred practice of this invention. Representative process oils are Coprol Oil B (Atlantic Refining Company), Circo Light Processing Oil (Sun Oil Company, and Sovaloid N (Socony Mobil Oil Co.). Coprol Oil B has an A.P.I gravity at 60 F. of 23.5, and the S.S.U. Viscosity is at 100 F. and 39 at 210 F.
The surface-active agent employed is one which is capable of effectively emulsifying the oil and bringing about compatibility with the latex; in the sulfur-paste mixture, the amount of emulsifyer employed for this purpose generally falling into a range. of from about 0.025 to 0.25 part, per 100 parts of sulfur, or, expressed otherwise, per single part of oil. Representative einul sifying agents'of the anionic. type which may be successfully employed in a practice of this invention include various alkyl aryl sulfonates such as Nacconol NRSF (Allied Chemical and Dye corporation), Tamol N (Rohm and Haas Company), Nekal BX-78 (General Aniline and Film Corporation), petroleum sulfonates such as Petronate HL (L. Sonneborn Sons, Inc.), as well as fatty acid sulfates such as Duponol ME (du Pont Co.) and Orvus W A Paste (Proctor and Gamble Company). Also satisfactory are certain emulsifiers of the non-ionic type, e.g., Atlas 1256, a polyoxyethylene sorbitol ester of a higher fatty acid, as marketed by Atlas Powder Company, and Triton X-100, an alkyl aryl polyether alcohol, as marketed by Rohm and Haas Co.
Storage stability test Sulfur 100 parts, emulsifier 0.1 part, plusindicated amounts of rubber and oil.
Percent fines produced at indicated storage condition.
Room Temperature 0 C 52 0. Oil Ruhr. When Cont Cont Made 1 Mo. v 2 M0. 3 Mo. 1 Mo. 2 Mo. 3 Mo. 1 Mo 3 Mo. 3 Mo.
Having selected the particular sulfur product and the additives to be employed, the recommended practice is to add sufficient water to the mixture of sulfur and additives to form a cohesive agglomerate, or heavy paste which can then be divided by a practice of conventional extrusion or screening methods into small pieces having the shape desired in the finished pellet. In general, the quantity of water required is of the order of 15-25 parts per 100 parts of sulfur. These wet, shaped elements are then dried at any appropriate temperature, good results having been obtained at temperature levels of 50, 70 and 90 C. Experience has shown that at any given temperature, the drying time is the same regardless of the rubber latex content within limits of 0.1 to 1.0 part thereof. Further, for those samples of like rubber content, no difference in physical property or stability were noted with variation in drying temperature. In most instances the finished pellets were observed to have a residual water content of less than 0.05 percent.
The nature of the present invention will be more fully understood by reference to the data presented in the following example which is set forth by way of illustration.
EXAMPLE In this operation pastes were prepared containing water parts), rubber-makers sulfur (100 parts), emulsifier (Atlas 1256) 0.1 part, oil (Coprol ()il B) 1.0 part, and rubber latex (either Pliolite Latex 2105 or Polyco 397-70 NS, both 70:30 butadiene-styrene rubbers) in varying proportions, i.e., 0.1, 0.25, 0.5 and 1.0, respectively. These parts by weight of the latex are on a dry weight basis and do not take into account the amount of water (about 60 percent) and other non-rubber materials present in the commercial product. As a control,
From the foregoing table it will be seen that amounts of rubber as small as 0.1 part impart stability characteristics to the pellets far superior to those observed in the absence of any rubber component. However, appreciably better results are obtained at the 0.25l part rubber level. Further, it can be seen that the combination of rubber latex and oil gives a product of high order stability; contrast this with the products obtained with either rubber latex or oil alone.
The amount of fines produced from pellets dried at 50 C. and 70 C. was substantially the same as from pellets dried at 90 C.
All the rubber containing pellets made in the foregoing example were found to be capable of smearing out and v dispersing readily in a rubber mixture as the same was certain batches were also prepared in which the rubber latex ingredient was omited.
The various paste compositions prepared were forced through an 8-mesh screen, the extrudate being cut from the screen and allowed to drop in a pan. The pan was then oscillated in a circular motion, and within several moments spherical or oval pellets apuproximately diameter were formed. These wet pellets were then dried at a temperature of 90 C.
To evaluate the stability of the resulting dried pellets, a portion was tested in its freshly prepared condition, while others were stored for a period of from one to three months, some at room temperature, others at 0 C., and others at approximately 50 C. At the end of being milled. Further, it was observed that the dispersion of sulfur in the resulting rubber product was better than that which could otherwise be obtained by using just the powdered sulfur from which the pellets were made.
As employed herein and in the claims, the terms "rubber and rubber latex are employed somewhat interchangeably, reference being had, in any event, to a product formed by the addition of a rubber latex material, as described above.
We claim:
1. A pelleted sulfur product comprising predominantly sulfur and containing from about 0.1 to 1.25 parts rub ber per parts sulfur, said rubber being selected from the group consisting of natural rubber, butadiene-acrylonitrile copolymers, butadiene-styrene rubbers, rubbery chloroprene polymers and isobutylene-isoprene co-polymers and mixtures thereof, from 0.025 to 0.25 part of a surface active agent selected from the group consisting of anionic and non-ionic surface active agents per 100 parts sulfur and at least 0.25 part hydrocarbon oil per 100 parts sulfur, all parts being by weight.
2. A pelleted sulfur product containing from about 0.1 to 1.25 parts of rubber per 100 parts sulfur, said rubber being selected from the group consisting of natural rubber, butadiene-acrylonitrile co-polymers, butadiene-styreue rubbers, rubbery chloroprene polymers and isobutylene-isoprene co-polymers, and mixtures thereof and from 0.025 to 0.25 part of a surface active agent selected from the group consisting of anionic and non-ionic surface active agents per 100 parts of sulfur and 0.25 to 1.5 parts of a hydrocarbon oil per 100 parts of sulfur, all parts being by weight.
3. The product of claim 2 wherein the rubber conten is from 0.25 to 1 part per 100 parts sulfur.
4. The product of claim 2 wherein the rubber is a synthetic butadiene-styrene product present in an amount of from 0.25 to 1 part per 100 parts sulfur.
5. The product of claim 2 wherein the hydrocarbon oil is a mineral oil.
6. A process for the production of sulfur in the form of pellets having good plasticity and stability characteristics, which comprises admixing 100 parts of powdered sulfur, 0.1 to 1.25 parts rubber latex, said latex being selected from the group consisting of natural rubber, butadiene-acrylonitrile co-polymers, butadiene-styrene rubbers, rubbery chlorcprene polymers and isobutylene-isoprene co-polymers, and mixtures thereof, 0.25 to 1.5 parts hydrocarbon oil and a sufiicient amount of a surface active agent selected from the group consisting of anionic and non-ionic surface active agents to emulsify the oii and with water in amount necessary to form a paste; forming References Cited in the file of this patent UNITED STATES PATENTS 1,871,038 Cadwell Aug. 9, 1932 2,069,710 Missbach Feb. 2, 1937 2,640,088 Glenn et a1 May 26, 1953 OTHER REFERENCES Hancock: Industrial & Eng. Chem, November 1954,
vol. 46, No. 11, pp. 2431-2434.

Claims (1)

1. A PELLETED SULFUR PRODUCT COMPRISING PREDOMINANTLY SULFUR AND CONTAINING FROM ABOUT 0.1 TO 1.25 PARTS RUBBER PER 100 PARTS SULFUR, SAID RUBBER BEING SELECTED FROM THE GROUP CONSISTING OF NATURAL RUBBER, BUTADIENE-ACRYLONITRILE COPOLYMERS, BUTADIENE-STYRENE RUBBERS, RUBBERY CHLOROPRENE POLYMERS AND ISOBUTYLENE-ISOPRENE CO-POLYMERS AND MIXTURES THEREOF, FROM 0.025 TO 0.25 PART OF A SURFACE ACTIVE AGENT SELECTED FROM THE GROUP CONSISTING OF ANIONIC AND NON-IONIC SURFACE ACTIVE AGENTS PER 100 PARTS SULFUR AND AT LEAST 0.25 PART HYDROCARBON OIL PER 100 PARTS SULFUR, ALL PARTS BEING BY WEIGHT.
US724258A 1958-03-27 1958-03-27 Pelletized sulfur Expired - Lifetime US3012985A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US724258A US3012985A (en) 1958-03-27 1958-03-27 Pelletized sulfur

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US724258A US3012985A (en) 1958-03-27 1958-03-27 Pelletized sulfur

Publications (1)

Publication Number Publication Date
US3012985A true US3012985A (en) 1961-12-12

Family

ID=24909689

Family Applications (1)

Application Number Title Priority Date Filing Date
US724258A Expired - Lifetime US3012985A (en) 1958-03-27 1958-03-27 Pelletized sulfur

Country Status (1)

Country Link
US (1) US3012985A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3236799A (en) * 1962-04-24 1966-02-22 Grace W R & Co Process of preparing a rubber and oil latex with sulfur
US3979316A (en) * 1972-09-27 1976-09-07 Kali-Chemie Aktiengesellschaft Pelleted sulfur compositions and processes for their production
US4032469A (en) * 1972-09-27 1977-06-28 Kali-Chemie Aktiengesellschaft Pelleted sulfur compositions
US4092285A (en) * 1976-07-30 1978-05-30 Wyrough And Loser, Inc. Encapsulation of critical chemicals
JPS6119643A (en) * 1984-07-07 1986-01-28 Sanshin Kagaku Kogyo Kk Modifier for dispersion of insoluble sulfur in rubber
US4639508A (en) * 1980-01-16 1987-01-27 Toyo Soda Manufacturing Co., Ltd. Process for producing granular composition of ethylenethiourea-chloroprene rubber
FR2599018A1 (en) * 1986-05-22 1987-11-27 Raffineries Soufre Reunies Sulphur granules and process for their manufacture
WO2004005386A1 (en) * 2002-07-08 2004-01-15 Basf Aktiengesellschaft Method for vulcanizing caoutchouc or latex by applying a mixture of sulfur and a complexing agent

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1871038A (en) * 1931-11-27 1932-08-09 Naugatuck Chem Co Vulcanization of rubber and similar materials
US2069710A (en) * 1934-02-26 1937-02-02 San Francisco Sulphur Company Prepared sulphur
US2640088A (en) * 1950-01-06 1953-05-26 Us Rubber Co Vulcanization accelerators

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1871038A (en) * 1931-11-27 1932-08-09 Naugatuck Chem Co Vulcanization of rubber and similar materials
US2069710A (en) * 1934-02-26 1937-02-02 San Francisco Sulphur Company Prepared sulphur
US2640088A (en) * 1950-01-06 1953-05-26 Us Rubber Co Vulcanization accelerators

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3236799A (en) * 1962-04-24 1966-02-22 Grace W R & Co Process of preparing a rubber and oil latex with sulfur
US3979316A (en) * 1972-09-27 1976-09-07 Kali-Chemie Aktiengesellschaft Pelleted sulfur compositions and processes for their production
US4032469A (en) * 1972-09-27 1977-06-28 Kali-Chemie Aktiengesellschaft Pelleted sulfur compositions
US4092285A (en) * 1976-07-30 1978-05-30 Wyrough And Loser, Inc. Encapsulation of critical chemicals
US4639508A (en) * 1980-01-16 1987-01-27 Toyo Soda Manufacturing Co., Ltd. Process for producing granular composition of ethylenethiourea-chloroprene rubber
EP0170104A1 (en) * 1984-07-07 1986-02-05 Sanshin Kagaku Kogyo Co., Ltd. Rubber dispersive agent for insoluble sulphur and process of preparing same
JPS6119643A (en) * 1984-07-07 1986-01-28 Sanshin Kagaku Kogyo Kk Modifier for dispersion of insoluble sulfur in rubber
US4737542A (en) * 1984-07-07 1988-04-12 Sanshin Kagaku Kogyo Co., Ltd. Vulcanizing composition
JPH0464544B2 (en) * 1984-07-07 1992-10-15 Sanshin Kagaku Kogyo Kk
FR2599018A1 (en) * 1986-05-22 1987-11-27 Raffineries Soufre Reunies Sulphur granules and process for their manufacture
WO2004005386A1 (en) * 2002-07-08 2004-01-15 Basf Aktiengesellschaft Method for vulcanizing caoutchouc or latex by applying a mixture of sulfur and a complexing agent
US20050288448A1 (en) * 2002-07-08 2005-12-29 Basf Aktiengesellschaft Method for vulcanizing caoutchouc or latex by applying a mixture of sulfur and a complexing agent
US7132482B2 (en) 2002-07-08 2006-11-07 Basf Aktiengesellschaft Method for vulcanizing caoutchouc or latex by applying a mixture of sulfur and a complexing agent

Similar Documents

Publication Publication Date Title
US3012985A (en) Pelletized sulfur
US2427238A (en) Carbon black pellets
US2640088A (en) Vulcanization accelerators
US3431214A (en) Compacted sulfur and method of producing same
US3235529A (en) Free flowing polystyrene powders containing 10-40% plasticizer
US4097558A (en) Resin blend for making plastisols and organosols
US2847710A (en) Method of improving fluid properties of finely divided materials
US4335033A (en) Eraser and process for its manufacture
US2888444A (en) Process for pelletizing dry rubber accelerators
US2771458A (en) Solutions of rubbery polymers from particles of uniform diameter
PT95840A (en) PROCESS FOR THE PREPARATION OF COMPOSITIONS FOR COATING HUMID RUBBER PARTICLES AND PRODUCING RUBBER RUBBER BURGLARS
US2411470A (en) Composition comprising vermiculite and a thermoplastic resin
EP0248162B1 (en) Expandable gel-forming and heat-vulcanizable composition for preparing a latex foam
US2962456A (en) Process for preparing foamed styrene polymers containing an inorganic pigment
US2315924A (en) Process for preventing rubber objects from sticking together and improving the quality and durability of raw rubber in a divided state
US2933464A (en) Pelletized acceleration containing polyisobutylene
US4171428A (en) Method for manufacturing plastisol resins using spray-drying
US2613189A (en) Cellular material and blowing agent therefor
US2278833A (en) Rubberlike composition containing neoprene and polyvinyl chloride
US5475059A (en) Method of achieving superior dispersions of polymeric sulfur and products thereof
US2858283A (en) Method of making textile fiber drafting elements containing animal glue, a rubber, and a surface-active material
US3809567A (en) Polychloroprene rubbers
US2432221A (en) Molding materials
US3073789A (en) Stable non-adhesive butadiene-styrene crumb rubber containing a silicone oxide condensation polymer and finely divided silica and process for making same
GB987769A (en) Foamed polymers and process for preparing same